Canonical Allele Identifier: CA2336453939
Gene: BCKDHA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41410980G= , CM000681.2:g.41410980G= GRCh38
NC_000019.9:g.41916885G= , CM000681.1:g.41916885G= GRCh37
NC_000019.8:g.46608725G= NCBI36
NG_013004.1:g.18192G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000269980.7:c.346G= MANE Select ENSP00000269980.2:p.Asp116=
ENST00000269980.6:c.346G= ENSP00000269980.2:p.Asp116=
ENST00000457836.6:c.280G= ENSP00000416000.2:p.Asp94=
ENST00000538423.5:n.472G=
ENST00000540732.3:c.448G= ENSP00000443246.1:p.Asp150=
ENST00000541315.1:c.153G=
ENST00000542943.5:c.288+164G= ENSP00000440345.1:n.288+164G=
ENST00000595085.5:c.346G= ENSP00000471150.2:p.Asp116=
NM_000709.3:c.346G= NP_000700.1:p.Asp116=
NM_001164783.1:c.346G= NP_001158255.1:p.Asp116=
NM_000709.4:c.346G= MANE Select NP_000700.1:p.Asp116=
NM_001164783.2:c.346G= NP_001158255.1:p.Asp116=